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CAS No. : | 343788-69-2 | MDL No. : | MFCD03265497 |
Formula : | C11H22N2O2 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | DMBKWEHXTOCLTC-UHFFFAOYSA-N |
M.W : | 214.31 | Pubchem ID : | 11310432 |
Synonyms : |
|
Signal Word: | Warning | Class: | |
Precautionary Statements: | P280-P305+P351+P338-P310 | UN#: | |
Hazard Statements: | H302-H315-H319-H332-H335 | Packing Group: | |
GHS Pictogram: |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
67% | j00219J A vial was charged with DCE (10 mL), <strong>[372120-55-3]3-bromo-4-(trifluoromethyl)benzaldehyde</strong> (252 mg, 1.00 mmol, 1.00 equiv), t-butyl 4-amino-4-methylpiperidine-1-carboxylate (214 mg, 1.00 mmol,1.00 equiv), and triethylamine (303 mg, 2.99 mmol, 3.00 equiv). The resulting solution was stirred for 1 h at room temperature, then sodium triacetoxyborohydride (636 mg, 3.00 mmol, 3.00 equiv) was added. The mixture was stirred overnight at room temperature and quenched with water (10 mL), as described in Example 1, Step 6. The residue was chromatographed on a silica gel column to provide 300 mg (67% yield) of t-butyl 4-((3-bromo-4-(trifluoromethyl)benzyl)amino)-4- methylpiperidine-1-carboxylate as a yellow oil. LCMS (ESI, m/z): 451 [M+H]. |
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